Structure Information
Structure

Compound Identification

SMILES

C[C@]1(O)[C@@H](O)[C@H](CO)O[C@@H]1N1C=C(C(N)=O)C2=C1N=C(N)N=C2N

InChIKey

InChIKey=HSILALYSUFKBEL-VKDYPGQGSA-N

Formula

C13H18N6O5

Mass

338.324

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrrolopyrimidine nucleosides and nucleotides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Pyrrolopyrimidine nucleosides and nucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Pyrrolopyrimidine ribonucleoside - Glycosyl compound - N-glycosyl compound - Pyrrolo[2,3-d]pyrimidine - Pyrimidinecarboxamide - Pyrrolopyrimidine - Pyrrole-3-carboxamide - Pyrrole-3-carboxylic acid or derivatives - Aminopyrimidine - Monosaccharide - Pyrimidine - Substituted pyrrole - Imidolactam - Oxolane - Pyrrole - Tertiary alcohol - Heteroaromatic compound - Vinylogous amide - Secondary alcohol - 1,2-diol - Amino acid or derivatives - Primary carboxylic acid amide - Carboxamide group - Oxacycle - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Hydrocarbon derivative - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Primary alcohol - Primary amine - Organic oxide - Amine - Alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as pyrrolopyrimidine nucleosides and nucleotides. These are nucleoside derivatives containing a ribose derivative which is n-glycosylated to a pyrrolopyrimidine. Also called deazapurine nucleosides, they are analogs of purine nucleosides with the N atom of the purine being replaced by a C atom at position 7.

External Descriptors

Not available

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